Synthesis of mixed-ligand cobalt complexes and their applications in high cis-1,4-selective butadiene polymerization
摘要:
Incomplete oxidation of (N-di-tert-butylphosphino)-6-(2-methyl-2'H-benzoimidazole)-2-aminepyridine dichlorocobalt ((PNCoCl2)-Co-3) in DMF results in a unique co-crystal I formed with three parts including DMF, unit A and unit B complex with Co1 and Co2, respectively (PN3 ligand in unit A: (N-di-tertbutylphosphino)-6-(2'-methyl-2'H-benzoimidazole)-2-aminepyridine, and O=PN3 ligand in unit B: (N-di-tert-butylphosphinoxide)-6-(2'-methyl-2'H-benzoimidazole)-2-aminepyridine), with 1:1:1 molar ratio. Co1 and Co2 complexes both display a five-coordinated distorted-square-pyramidal geometry around the metal center. The Co1 center is coordinated with PN3 ligand via two N atoms from pyridine, benzoimidazole moiety as well as one P atom, and the Co2 center is coordinated with the oxidized ligand O=PN3 via two N atoms from pyridine, benzoimidazole moiety as well as one O atom from DMF molecule, while the oxidized phosphine moiety (O=P) being excluded from the coordination sphere. Activated with AlEt2Cl, the co-crystallized complexes I are able to actively convert butadiene to polybutadiene, affording cis-1,4 polybutadiene with cis-1,4 unit up to 95.5-97.8% and number average molecular weight of cal. 10(5) g/mol. The high cis-1,4 selectivity and monomodal GPC curve of resultant polymer imply that the identical active species generated from two distinctive cobalt centers. (C) 2015 Elsevier B.V. All rights reserved.
Synthesis of mixed-ligand cobalt complexes and their applications in high cis-1,4-selective butadiene polymerization
摘要:
Incomplete oxidation of (N-di-tert-butylphosphino)-6-(2-methyl-2'H-benzoimidazole)-2-aminepyridine dichlorocobalt ((PNCoCl2)-Co-3) in DMF results in a unique co-crystal I formed with three parts including DMF, unit A and unit B complex with Co1 and Co2, respectively (PN3 ligand in unit A: (N-di-tertbutylphosphino)-6-(2'-methyl-2'H-benzoimidazole)-2-aminepyridine, and O=PN3 ligand in unit B: (N-di-tert-butylphosphinoxide)-6-(2'-methyl-2'H-benzoimidazole)-2-aminepyridine), with 1:1:1 molar ratio. Co1 and Co2 complexes both display a five-coordinated distorted-square-pyramidal geometry around the metal center. The Co1 center is coordinated with PN3 ligand via two N atoms from pyridine, benzoimidazole moiety as well as one P atom, and the Co2 center is coordinated with the oxidized ligand O=PN3 via two N atoms from pyridine, benzoimidazole moiety as well as one O atom from DMF molecule, while the oxidized phosphine moiety (O=P) being excluded from the coordination sphere. Activated with AlEt2Cl, the co-crystallized complexes I are able to actively convert butadiene to polybutadiene, affording cis-1,4 polybutadiene with cis-1,4 unit up to 95.5-97.8% and number average molecular weight of cal. 10(5) g/mol. The high cis-1,4 selectivity and monomodal GPC curve of resultant polymer imply that the identical active species generated from two distinctive cobalt centers. (C) 2015 Elsevier B.V. All rights reserved.
A robust NNP‐type ruthenium (II) complex for alcohols dehydrogenation to esters and pyrroles
作者:Huining Chai、Guangyao Zhang、Weiqiang Tan、Jiping Ma
DOI:10.1002/aoc.5367
日期:2020.2
(II) complex bearing pyridyl‐based benzimidazole‐phosphine tridentate NNP ligand was synthesized and structurally characterized by NMR, IR. The complex can efficiently and selectively catalyze the acceptorless dehydrogenation of primary alcohols to esters under relatively mild conditions and the synthesis of pyrroles by means of the reactions of secondary alcohols and β‐amino alcohols through acceptorless